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rs730880754

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880754(A;A)
Make rs730880754(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424131
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880754
ebirs730880754
HLIrs730880754
Exacrs730880754
Varsomers730880754
Maprs730880754
PheGenIrs730880754
hapmaprs730880754
1000 genomesrs730880754
hgdprs730880754
ensemblrs730880754
gopubmedrs730880754
geneviewrs730880754
scholarrs730880754
googlers730880754
pharmgkbrs730880754
gwascentralrs730880754
openSNPrs730880754
23andMers730880754
23andMe allrs730880754
SNP Nexus

SNPshotrs730880754
SNPdbers730880754
MSV3drs730880754
GWAS Ctlgrs730880754
Max Magnitude0
ClinVar
Risk rs730880754(A;A)
Alt rs730880754(A;A)
Reference rs730880754(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893340C>T
CLNSRC
CLNACC RCV000158562.2,